Lista de obras - Mark W Head - Dominio Público Uruguay

A case of protease sensitive prionopathy in a patient in the UK.

artículo científico publicado en 2009

A case of variably protease-sensitive prionopathy treated with doxycyclin

artículo científico publicado en 2015

A new index of agonal state for neurological disease

artículo científico publicado en 2011

A new prionopathy.

artículo científico publicado en 2008

A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature

artículo científico publicado en 2010

A prion protein epitope selective for the pathologically misfolded conformation

artículo científico publicado en 2003

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

artículo científico publicado en 2007

Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease.

artículo científico publicado en 2005

Advances in the development of a screening test for variant Creutzfeldt–Jakob disease

scientific article published on 01 February 2008

Ageing in the chick lens: in vitro studies.

artículo científico publicado en 1991

An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimens

artículo científico publicado en 2008

Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD.

artículo científico publicado en 2007

Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob disease

artículo científico publicado en 2006

Application of magnetic field–induced heat shock protein 70 for presurgical cytoprotection

artículo científico publicado en 1998

Biology and neuropathology of prion diseases

artículo científico publicado en 2008

Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2000

Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blot

artículo científico publicado en 2010

Coordinate and independent regulation of alpha B-crystallin and hsp27 expression in response to physiological stress.

artículo científico publicado en 1994

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

artículo científico publicado en 2016

Correlation of Polydispersed Prion Protein and Characteristic Pathology in the Thalamus in Variant Creutzfeldt-Jakob Disease: Implication of Small Oligomeric Species

artículo científico publicado en 2010

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease

artículo científico publicado en 2006

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

artículo científico publicado en 2006

Differential protein profiling as a potential multi-marker approach for TSE diagnosis

artículo científico publicado en 2009

Disease-associated prion protein is not detectable in human systemic amyloid deposits

artículo científico publicado en 2007

Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassay

artículo científico publicado en 2010

Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK.

artículo científico publicado en 2006

Effects of age and genetic growth rate on the crystallin composition of the chick lens.

artículo científico

Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay

artículo científico publicado en 2008

Electromagnetic field exposure induces rapid, transitory heat shock factor activation in human cells

scientific article published on 01 September 1997

Evaluation of urinary PrPSc as a diagnostic test for sporadic, variant, and familial CJD.

artículo científico publicado en 2005

Evidence for the extralenticular expression of members of the β-crystallin gene family in the chick and a comparison with δ-crystallin during differentiation and transdifferentiation

article

Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches.

artículo científico publicado en 2014

Expression of the chicken cysteine-rich fibroblast growth factor receptor (CFR) during embryogenesis and retina development

artículo científico publicado en 1996

Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice

artículo científico publicado en 1998

Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt-Jakob disease brain reference materials

artículo científico publicado en 2009

Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potential

artículo científico publicado en 2014

Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies

artículo científico publicado en 2014

Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitro.

artículo científico publicado en 2011

Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease

artículo científico publicado en 2008

Human prion diseases: Molecular, cellular and population biology ⬇️

artículo científico publicado el 20 de enero de 2013

Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner

artículo científico publicado en 2017

Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes

artículo científico publicado en 2013

Immunohistochemistry for the prion protein: comparison of different monoclonal antibodies in human prion disease subtypes.

artículo científico publicado en 2002

In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc.

artículo científico publicado en 2007

Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium

artículo científico publicado en 2008

Investigation of prion diseases.

artículo científico publicado en 2001

Laboratory diagnosis of variant Creutzfeldt-Jakob disease.

artículo científico publicado en 2000

Localization of delta-crystallin RNA during lens morphogenesis and differentiation in the normal and talpid3 chick embryo

artículo científico publicado el 1 de septiembre de 1992

Macular holes: migratory gaps and vitreous as obstacles to glial closure

artículo científico publicado en 1997

Molecular barriers to zoonotic transmission of prions

artículo científico publicado en 2014

Molecular model of prion transmission to humans

artículo científico publicado en 2009

Motif-grafted antibodies containing the replicative interface of cellular PrP are specific for PrPSc

artículo científico publicado en 2004

Myc-mediated transactivation of HSP70 expression following exposure to magnetic fields

scientific article published on 01 May 1998

Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.

artículo científico publicado en 2004

Neuropathology of variant Creutzfeldt-Jakob disease.

artículo científico publicado en 2002

No major change in vCJD agent strain after secondary transmission via blood transfusion

artículo científico publicado en 2008

Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patients.

artículo científico publicado en 2009

Pathological and biochemical investigation of a woman diagnosed with genetic Creutzfeldt-Jakob disease shortly after parturition

artículo científico publicado en 2015

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study

artículo científico publicado en 2004

Phenotypic variability in human prion diseases.

artículo científico publicado en 2005

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

artículo científico publicado en 2004

Predicting susceptibility and incubation time of human-to-human transmission of vCJD.

artículo científico publicado en 2006

Prion protein accumulation and neuroprotection in hypoxic brain damage

artículo científico publicado en 2004

Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease

artículo científico publicado en 2003

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

artículo científico publicado en 2004

Production and Characterization of a Panel of Monoclonal Antibodies Against Native Human Cellular Prion Protein

artículo científico publicado en 2009

Properties of the cellular prion protein expressed in Xenopus oocytes

artículo científico publicado en 2002

Purification of normal cellular prion protein from human platelets and the formation of a high molecular weight prion protein complex following platelet activation

artículo científico publicado en 2005

RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissue.

artículo científico

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2012

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

artículo científico publicado en 2016

Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.

artículo científico

Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion

artículo científico publicado en 2011

Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease.

artículo científico publicado en 2004

Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotype.

artículo científico publicado en 2001

Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?

artículo científico publicado en 2009

Sporadic Creutzfeldt-Jakob disease: further twists and turns in a convoluted protein

artículo científico publicado en 2006

Standards for the assay of Creutzfeldt-Jakob disease specimens

artículo científico publicado en 2004

Suppression of fibroblast growth factor 2 expression by antisense oligonucleotides inhibits embryonic chick neural retina cell differentiation and survival in vivo ⬇️

artículo científico publicado el 1 de mayo de 1998

The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

artículo científico publicado en 2016

The application of in vitro cell-free conversion systems to human prion diseases

artículo científico publicado en 2010

The contribution of different prion protein types and host polymorphisms to clinicopathological variations in Creutzfeldt-Jakob disease

artículo científico

The prion protein protease sensitivity, stability and seeding activity in variably protease sensitive prionopathy brain tissue suggests molecular overlaps with sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2014

The transmissible spongiform encephalopathies: pathogenic mechanisms and strategies for therapeutic intervention

artículo científico publicado en 2001

Transcription regulation of alpha B-crystallin in astrocytes: analysis of HSF and AP1 activation by different types of physiological stress

artículo científico publicado en 1996

Transmissions of variant Creutzfeldt-Jakob disease from brain and lymphoreticular tissue show uniform and conserved bovine spongiform encephalopathy-related phenotypic properties on primary and secondary passage in wild-type mice

artículo científico publicado en 2009

Transplantation of ocular tissue from a donor with sporadic Creutzfeldt-Jakob disease

artículo científico publicado en 2006

UK Iatrogenic Creutzfeldt-Jakob disease: investigating human prion transmission across genotypic barriers using human tissue-based and molecular approaches

artículo científico publicado en 2016

Uptake and degradation of protease-sensitive and -resistant forms of abnormal human prion protein aggregates by human astrocytes

artículo científico publicado en 2014

Variably protease-sensitive prionopathy in a PRNP codon 129 heterozygous UK patient with co-existing tau, α synuclein and Aβ pathology

artículo científico publicado en 2010

Variably protease-sensitive prionopathy in the UK: a retrospective review 1991-2008.

artículo científico publicado en 2013

Variant CJD. 18 years of research and surveillance

artículo científico publicado en 2014

Variant Creutzfeldt-Jakob disease

scientific article published on 01 March 2003

Variant Creutzfeldt-Jakob disease in France and the United Kingdom: Evidence for the same agent strain

artículo científico publicado en 2009

Variation in concentration of prion protein in the peripheral blood of patients with variant and sporadic Creutzfeldt-Jakob disease detected by dissociation enhanced lanthanide fluoroimmunoassay and flow cytometry

artículo científico publicado en 2005

vCJD and the gut: implications for endoscopy

artículo científico publicado en 2007

βB2-Crystallin in the mammalian retina

scientific article published on 01 October 1995

Lista de obras de Mark W Head

A case of protease sensitive prionopathy in a patient in the UK.

A case of variably protease-sensitive prionopathy treated with doxycyclin

A new index of agonal state for neurological disease

A new prionopathy.

A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature

A prion protein epitope selective for the pathologically misfolded conformation

Abnormal prion protein in the pituitary in sporadic and variant Creutzfeldt-Jakob disease

Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease.

Advances in the development of a screening test for variant Creutzfeldt–Jakob disease

Ageing in the chick lens: in vitro studies.

An antibody to the aggregated synthetic prion protein peptide (PrP106-126) selectively recognizes disease-associated prion protein (PrP) from human brain specimens

Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD.

Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein in brain, spleen and blood specimens from patients with variant Creutzfeldt-Jakob disease

Application of magnetic field–induced heat shock protein 70 for presurgical cytoprotection

Biology and neuropathology of prion diseases

Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob disease

Comparison of the level, distribution and form of disease-associated prion protein in variant and sporadic Creutzfeldt-Jakob diseased brain using conformation-dependent immunoassay and Western blot

Coordinate and independent regulation of alpha B-crystallin and hsp27 expression in response to physiological stress.

Correction: The Distribution of Prion Protein Allotypes Differs Between Sporadic and Iatrogenic Creutzfeldt-Jakob Disease Patients

Correlation of Polydispersed Prion Protein and Characteristic Pathology in the Thalamus in Variant Creutzfeldt-Jakob Disease: Implication of Small Oligomeric Species

Detection and localization of PrPSc in the skeletal muscle of patients with variant, iatrogenic, and sporadic forms of Creutzfeldt-Jakob disease

Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease

Differential protein profiling as a potential multi-marker approach for TSE diagnosis

Disease-associated prion protein is not detectable in human systemic amyloid deposits

Distinct stability states of disease-associated human prion protein identified by conformation-dependent immunoassay

Dura mater-associated Creutzfeldt-Jakob disease: experience from surveillance in the UK.

Effects of age and genetic growth rate on the crystallin composition of the chick lens.

Effects of human PrPSc type and PRNP genotype in an in-vitro conversion assay

Electromagnetic field exposure induces rapid, transitory heat shock factor activation in human cells

Evaluation of urinary PrPSc as a diagnostic test for sporadic, variant, and familial CJD.

Evidence for the extralenticular expression of members of the β-crystallin gene family in the chick and a comparison with δ-crystallin during differentiation and transdifferentiation

Exploring the zoonotic potential of animal prion diseases: in vivo and in vitro approaches.

Expression of the chicken cysteine-rich fibroblast growth factor receptor (CFR) during embryogenesis and retina development

Fatal encephalopathy with astrocyte inclusions in GFAP transgenic mice

Further characterisation of the prion protein molecular types detectable in the NIBSC Creutzfeldt-Jakob disease brain reference materials

Genotype-dependent molecular evolution of sheep bovine spongiform encephalopathy (BSE) prions in vitro affects their zoonotic potential

Gerstmann-Straüssler-Scheinker disease: novel PRNP mutation and VGKC-complex antibodies

Human embryonic stem cells rapidly take up and then clear exogenous human and animal prions in vitro.

Human platelets as a substrate source for the in vitro amplification of the abnormal prion protein (PrP) associated with variant Creutzfeldt-Jakob disease

Human prion diseases: Molecular, cellular and population biology ⬇️

Human stem cell-derived astrocytes replicate human prions in a PRNP genotype-dependent manner

Human tonsil-derived follicular dendritic-like cells are refractory to human prion infection in vitro and traffic disease-associated prion protein to lysosomes

Immunohistochemistry for the prion protein: comparison of different monoclonal antibodies in human prion disease subtypes.

In vitro amplification and detection of variant Creutzfeldt-Jakob disease PrPSc.

Inter-laboratory assessment of PrPSc typing in creutzfeldt-jakob disease: a Western blot study within the NeuroPrion Consortium

Investigation of prion diseases.

Laboratory diagnosis of variant Creutzfeldt-Jakob disease.

Localization of delta-crystallin RNA during lens morphogenesis and differentiation in the normal and talpid3 chick embryo

Macular holes: migratory gaps and vitreous as obstacles to glial closure

Molecular barriers to zoonotic transmission of prions

Molecular model of prion transmission to humans

Motif-grafted antibodies containing the replicative interface of cellular PrP are specific for PrPSc

Myc-mediated transactivation of HSP70 expression following exposure to magnetic fields

Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.

Neuropathology of variant Creutzfeldt-Jakob disease.

No major change in vCJD agent strain after secondary transmission via blood transfusion

Panencephalopathic Creutzfeldt-Jakob disease in the Netherlands and the UK: clinical and pathological characteristics of nine patients.

Pathological and biochemical investigation of a woman diagnosed with genetic Creutzfeldt-Jakob disease shortly after parturition

Peripheral tissue involvement in sporadic, iatrogenic, and variant Creutzfeldt-Jakob disease: an immunohistochemical, quantitative, and biochemical study

Phenotypic variability in human prion diseases.

Preclinical vCJD after blood transfusion in a PRNP codon 129 heterozygous patient

Predicting susceptibility and incubation time of human-to-human transmission of vCJD.

Prion protein accumulation and neuroprotection in hypoxic brain damage

Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease

Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.

Production and Characterization of a Panel of Monoclonal Antibodies Against Native Human Cellular Prion Protein

Properties of the cellular prion protein expressed in Xenopus oocytes

Purification of normal cellular prion protein from human platelets and the formation of a high molecular weight prion protein complex following platelet activation

RNA integrity in post mortem human variant Creutzfeldt-Jakob disease (vCJD) and control brain tissue.

Real time quaking-induced conversion analysis of cerebrospinal fluid in sporadic Creutzfeldt-Jakob disease

Relative Abundance of apoE and Aβ1-42 Associated with Abnormal Prion Protein Differs between Creutzfeldt-Jakob Disease Subtypes

Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain.

Sensitive and specific detection of sporadic Creutzfeldt-Jakob disease brain prion protein using real-time quaking-induced conversion

Specificity of lymphoreticular accumulation of prion protein for variant Creutzfeldt-Jakob disease.

Sporadic Creutzfeldt-Jakob disease in a young Dutch valine homozygote: atypical molecular phenotype.

Sporadic Creutzfeldt-Jakob disease: discrete subtypes or a spectrum of disease?

Sporadic Creutzfeldt-Jakob disease: further twists and turns in a convoluted protein

Standards for the assay of Creutzfeldt-Jakob disease specimens

Suppression of fibroblast growth factor 2 expression by antisense oligonucleotides inhibits embryonic chick neural retina cell differentiation and survival in vivo ⬇️